Multiple-Filling-Induced Full-Spectrum Phonon Scattering and Band Convergence Leading to High-Performance n-Type Skutterudites
Source abstract
Abstract
Filling guest atoms into the nanovoids of skutterudite compounds provides effective scattering for low-frequency phonons to reduce the lattice thermal conductivity. However, it is still difficult to simultaneously realize the full-spectrum phonon scattering and band engineering in the n-type skutterudites with higher thermoelectric performance. Here, we reveal that the combination of five types of element atoms in the lattice nanovoids brings about dense dislocations, abundant precipitated nanoparticles, and electronic band convergence in the n-type skutterudites. The Seebeck coefficient shows an increase with little deterioration on the carrier mobility due to the enhanced density of states near the Fermi level, leading to a 11% enhancement in the power factor at 823 K. The lattice thermal conductivity is significantly reduced to approach the glass limit due to the full-spectrum phonon scattering. As a result, a peak ZT value of about 1.7 at 823 K and an average ZT value of about 1.2 from 323 to 823 K are obtained. High thermoelectric performance combined with the structural optimization enables the simulated maximum energy conversion efficiency of the skutterudite module to reach up to 15.0%. Our finding opens a new dimension for doping atoms to achieve simultaneous optimization of electrical and thermal properties in polynary thermoelectric materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Thermal properties of materials · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Advanced Welding and Joining, Harbin Institute of Technology, Harbin 150001, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (65)
Show source-provided references
1. Rowe D. M. · 1995
2. Uher C. · 201610.1201/9781315197029 ↗
3. 10.1126/science.272.5266.132510.1126/science.272.5266.1325 ↗
4. 10.1103/physrevlett.95.18550310.1103/physrevlett.95.185503 ↗
5. 10.1021/ja111199y10.1021/ja111199y ↗
6. 10.1016/j.actamat.2009.03.01810.1016/j.actamat.2009.03.018 ↗
7. 10.1016/j.actamat.2013.09.03910.1016/j.actamat.2013.09.039 ↗
8. 10.1016/j.jallcom.2012.05.01110.1016/j.jallcom.2012.05.011 ↗
9. 10.1063/1.281567110.1063/1.2815671 ↗
10. 10.1063/1.305415810.1063/1.3054158 ↗
11. 10.1039/c6ta09092c10.1039/c6ta09092c ↗
12. 10.1007/s11664-012-2370-510.1007/s11664-012-2370-5 ↗
13. 10.1021/acsaem.9b0185110.1021/acsaem.9b01851 ↗
14. 10.1016/j.nanoen.2016.11.04110.1016/j.nanoen.2016.11.041 ↗
15. 10.1016/j.nanoen.2016.11.01610.1016/j.nanoen.2016.11.016 ↗
16. 10.1007/s11664-013-2886-310.1007/s11664-013-2886-3 ↗
17. 10.1103/physrevlett.118.24590110.1103/physrevlett.118.245901 ↗
18. 10.1016/j.nanoen.2018.02.00910.1016/j.nanoen.2018.02.009 ↗
19. 10.1016/j.actamat.2021.11679110.1016/j.actamat.2021.116791 ↗
20. 10.1016/j.actamat.2019.11.01010.1016/j.actamat.2019.11.010 ↗
21. 10.1016/j.actamat.2013.07.03210.1016/j.actamat.2013.07.032 ↗
22. 10.2320/matertrans.mf20194110.2320/matertrans.mf201941 ↗
23. 10.1016/j.nanoen.2017.03.01210.1016/j.nanoen.2017.03.012 ↗
24. 10.1038/ncomms1382810.1038/ncomms13828 ↗
25. 10.1038/ncomms551510.1038/ncomms5515 ↗
26. 10.1039/c8ta07445c10.1039/c8ta07445c ↗
27. 10.1002/aenm.20160258210.1002/aenm.201602582 ↗
28. 10.1016/j.actamat.2015.07.02710.1016/j.actamat.2015.07.027 ↗
29. 10.1038/nmat443010.1038/nmat4430 ↗
30. 10.1038/srep1464110.1038/srep14641 ↗
31. 10.1021/acs.chemmater.6b0450610.1021/acs.chemmater.6b04506 ↗
32. 10.1021/acs.chemmater.0c0451710.1021/acs.chemmater.0c04517 ↗
33. 10.1063/1.273742210.1063/1.2737422 ↗
34. 10.1016/j.jssc.2004.02.01010.1016/j.jssc.2004.02.010 ↗
35. 10.1016/j.actamat.2014.11.02210.1016/j.actamat.2014.11.022 ↗
36. 10.1016/j.jallcom.2018.10.00310.1016/j.jallcom.2018.10.003 ↗
37. 10.1088/0370-1298/68/12/30310.1088/0370-1298/68/12/303 ↗
38. Li J. C. M. · 1981 · 498
39. 10.1073/pnas.191913611710.1073/pnas.1919136117 ↗
40. 10.1016/j.actamat.2019.10.00710.1016/j.actamat.2019.10.007 ↗
41. 10.1021/acs.chemmater.8b0399410.1021/acs.chemmater.8b03994 ↗
42. 10.1016/j.jssc.2012.08.02510.1016/j.jssc.2012.08.025 ↗
43. 10.1021/acsami.0c0179810.1021/acsami.0c01798 ↗
44. 10.1103/physrevb.46.613110.1103/physrevb.46.6131 ↗
45. 10.1103/physrev.120.114910.1103/physrev.120.1149 ↗
46. 10.1073/pnas.151023111210.1073/pnas.1510231112 ↗
47. 10.1038/nature2366710.1038/nature23667 ↗
48. 10.1016/j.actamat.2017.09.04410.1016/j.actamat.2017.09.044 ↗
49. 10.1016/j.jallcom.2020.15797110.1016/j.jallcom.2020.157971 ↗
50. 10.1016/j.nanoen.2019.10419310.1016/j.nanoen.2019.104193 ↗
51. 10.1016/j.jallcom.2019.15227210.1016/j.jallcom.2019.152272 ↗
52. 10.1126/science.abe129210.1126/science.abe1292 ↗
53. 10.1002/aenm.20180211610.1002/aenm.201802116 ↗
54. 10.1007/s11664-013-2855-x10.1007/s11664-013-2855-x ↗
55. 10.3390/ma1305113010.3390/ma13051130 ↗
56. 10.1038/s41467-020-16508-x10.1038/s41467-020-16508-x ↗
57. 10.1016/j.actamat.2014.12.04210.1016/j.actamat.2014.12.042 ↗
58. 10.1039/c5ee02979a10.1039/c5ee02979a ↗
59. 10.1016/j.enconman.2015.03.11210.1016/j.enconman.2015.03.112 ↗
60. 10.1039/c6ee02467j10.1039/c6ee02467j ↗
61. 10.1016/j.energy.2016.07.03410.1016/j.energy.2016.07.034 ↗
62. 10.1007/s11664-012-1958-010.1007/s11664-012-1958-0 ↗
63. 10.1007/s11664-012-2241-010.1007/s11664-012-2241-0 ↗
64. 10.1002/aenm.20170179710.1002/aenm.201701797 ↗
65. 10.1007/s11664-013-2501-710.1007/s11664-013-2501-7 ↗